2-Methoxyruteacaprine

Details

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Internal ID 8243fb75-ddcb-43bf-8155-a1609598e702
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 18-methoxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15(20),16,18-octaen-14-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H15N3O2/c1-24-11-6-7-14-16(10-11)21-18-17-13(8-9-22(18)19(14)23)12-4-2-3-5-15(12)20-17/h2-7,10,20H,8-9H2,1H3
InChI Key JDYVBLKLNUFKBD-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C19H15N3O2
Molecular Weight 317.30 g/mol
Exact Mass 317.116426730 g/mol
Topological Polar Surface Area (TPSA) 57.70 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL312248
2-Methoxyrutecarprine
BDBM50131043
2-Methoxy-8,13-dihydro-7H-indolo[2'',3'':3,4]pyrido[2,1-b]quinazolin-5-one

2D Structure

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2D Structure of 2-Methoxyruteacaprine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.7987 79.87%
Blood Brain Barrier + 0.8879 88.79%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7942 79.42%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior + 0.6428 64.28%
BSEP inhibitior + 0.8802 88.02%
P-glycoprotein inhibitior - 0.5207 52.07%
P-glycoprotein substrate - 0.7563 75.63%
CYP3A4 substrate + 0.6556 65.56%
CYP2C9 substrate - 0.7813 78.13%
CYP2D6 substrate - 0.8230 82.30%
CYP3A4 inhibition + 0.6217 62.17%
CYP2C9 inhibition - 0.6155 61.55%
CYP2C19 inhibition - 0.6141 61.41%
CYP2D6 inhibition - 0.7773 77.73%
CYP1A2 inhibition + 0.9339 93.39%
CYP2C8 inhibition + 0.4536 45.36%
CYP inhibitory promiscuity + 0.7242 72.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6377 63.77%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9189 91.89%
Skin irritation - 0.8259 82.59%
Skin corrosion - 0.9569 95.69%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6030 60.30%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6397 63.97%
skin sensitisation - 0.9229 92.29%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6100 61.00%
Acute Oral Toxicity (c) II 0.5811 58.11%
Estrogen receptor binding + 0.9108 91.08%
Androgen receptor binding + 0.6824 68.24%
Thyroid receptor binding + 0.7390 73.90%
Glucocorticoid receptor binding + 0.7485 74.85%
Aromatase binding + 0.7537 75.37%
PPAR gamma + 0.7739 77.39%
Honey bee toxicity - 0.8887 88.87%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.8463 84.63%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.72% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.91% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.62% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 95.00% 93.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.54% 91.11%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 94.25% 92.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.21% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.91% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.70% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.98% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 91.84% 91.49%
CHEMBL2535 P11166 Glucose transporter 91.49% 98.75%
CHEMBL4208 P20618 Proteasome component C5 90.38% 90.00%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 89.52% 95.70%
CHEMBL1781 P11387 DNA topoisomerase I 88.94% 97.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.59% 86.33%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 88.01% 96.47%
CHEMBL4302 P08183 P-glycoprotein 1 87.60% 92.98%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.52% 93.65%
CHEMBL255 P29275 Adenosine A2b receptor 86.93% 98.59%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.77% 96.67%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.59% 97.36%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.89% 85.49%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 84.65% 96.39%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.76% 96.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.75% 91.71%
CHEMBL1907 P15144 Aminopeptidase N 83.69% 93.31%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 82.62% 95.53%
CHEMBL2056 P21728 Dopamine D1 receptor 81.02% 91.00%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 80.97% 85.00%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 80.36% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Trigonostemon bonianus
Vepris suaveolens

Cross-Links

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PubChem 135427256
LOTUS LTS0208429
wikiData Q104401536